Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Spain.
Gerencia de Atención Primaria Valladolid Oeste, Centro de Salud Delicias II, Valladolid, Spain; Servicio de Pediatría, Hospital clínico Universitario de Valladolid, Valladolid, Spain.
Int J Infect Dis. 2024 Jan;138:97-101. doi: 10.1016/j.ijid.2023.11.024. Epub 2023 Nov 24.
We aimed to analyze whether the expression of inflammatory and antiviral genes in respiratory syncytial virus (RSV)-infected infants' peripheral blood is associated with bronchiolitis progression.
We conducted a prospective study on 117 infants between 2015 and 2023. The expression levels of nine genes were quantified by quantitative polymerase chain reaction. Infants were classified according to their clinical evolution during hospital admission: (i) non-progression (n = 74), when the RSV bronchiolitis severity remained stable or improved; (ii) unfavorable progression (n = 43), when the RSV bronchiolitis severity increased. The association analysis was performed by logistic regression, adjusted by age, gender, prematurity, and RSV bronchiolitis severity in the emergency room.
Infants were 57.3% male, and the median age of the study population was 61 days. Thirty-five infants (30.7%) were admitted to the intensive care unit after hospital admission. Univariate logistic models showed that tumor necrosis factor (TNFα) and chemokine (C-C motif) ligand (CCL5) gene expression at baseline were inversely associated with unfavorable progression, which was confirmed by multivariate analyses: TNFα (adjusted odds ratio = 0.8 [95% confidence interval = 0.64-0.99], P-value = 0.038) and CCL5 (adjusted odds ratio = 0.76 [95% confidence interval = 0.62-0.93], P-value = 0.007).
An inadequate immune response to RSV, characterized by reduced gene expression levels of CCL5 and TNFα in peripheral blood, was associated with an unfavorable progression of RSV bronchiolitis.
分析呼吸道合胞病毒(RSV)感染婴儿外周血中炎症和抗病毒基因的表达是否与细支气管炎的进展有关。
我们对 2015 年至 2023 年间的 117 名婴儿进行了一项前瞻性研究。通过定量聚合酶链反应定量检测了 9 个基因的表达水平。根据婴儿住院期间的临床转归进行分类:(i)无进展(n=74),RSV 细支气管炎严重程度保持稳定或改善;(ii)不良进展(n=43),RSV 细支气管炎严重程度增加。采用逻辑回归分析,调整年龄、性别、早产和急诊室 RSV 细支气管炎严重程度。
婴儿中 57.3%为男性,研究人群的中位年龄为 61 天。35 名婴儿(30.7%)在住院后入住重症监护病房。单变量逻辑模型显示,基线时肿瘤坏死因子(TNFα)和趋化因子(C-C 基序)配体(CCL5)基因表达与不良进展呈负相关,多变量分析证实了这一点:TNFα(调整优势比=0.8 [95%置信区间=0.64-0.99],P 值=0.038)和 CCL5(调整优势比=0.76 [95%置信区间=0.62-0.93],P 值=0.007)。
外周血中 CCL5 和 TNFα 基因表达水平降低,表明 RSV 免疫反应不足,与 RSV 细支气管炎的不良进展有关。